Cited by 193Lipid metabolism and disordersParaoxonase enzyme and polymorphismsLipoproteins and Cardiovascular Health

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Hepatic lipase and dyslipidemia: interactions among genetic variants, obesity, gender and diet.

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Deeb, Samir S., Zambon, Alberto, Carr, Molly C., Ayyobi, Amir F., Brunzell, John D.·2003·Journal of Lipid Research

DOI 10.1194/jlr.r200017-jlr200

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Abstract

Hepatic lipase (HL) plays a central role in LDL and HDL remodeling. High HL activity is associated with small, dense LDL particles and with reduced HDL2 cholesterol levels. HL activity is determined by an HL gene promoter polymorphism, by gender (lower in premenopausal women), and by visceral obesity with insulin resistance. The activity is affected by dietary fat intake and selected medications. There is evidence for an interaction of the HL promoter polymorphism with visceral obesity, dietary fat intake, and with lipid-lowering medications in determining the level of HL activity. The dyslipidemia with high HL activity is a potentially proatherogenic lipoprotein profile in the metabolic syndrome, in Type 2 diabetes, and in familial combined hyperlipidemia.

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Authors: Deeb, S. S., Zambon, A., Carr, M. C., Ayyobi, A. F., & Brunzell, J. D.
Affiliations: University of Washington (US)
Corresponding author: Deeb, Samir S.
ORCID: Zambon, Alberto
Brunzell, John D.
Venue: Journal of Lipid Research
Publisher: Elsevier BV
Published: 2003-07
Volume: 44
Issue: 7
Pages: 1279-1286
ISSN: 0022-2275 (ISSN-L)
DOI: 10.1194/jlr.r200017-jlr200
OpenAlex: W2128832145
Cited by: 193
References: 80
Citations by year: 2026: 1 · 2025: 2 · 2024: 2 · 2023: 8 · 2022: 6 · 2021: 5 · 2020: 4 · 2019: 5 · 2018: 12 · 2017: 4 · 2016: 6 · 2015: 9 · 2014: 9 · 2013: 7 · 2012: 8
FWCI: 2.51
Type: journal article
Language: en
Open access: hybrid
doi.org
Licence: cc-by
www.elsevier.com/tdm/userlicense/1.0/ (tdm)
creativecommons.org/licenses/by/4.0/ (vor, 6267 d)
Locations: Journal of Lipid Research (publishedVersion, cc-by)
PubMed (publishedVersion)
DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders: National Heart, Lung, and Blood Institute (P01HL030086, HL3-0086, HL 64322, R01HL064322)
Topics: Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Lipid metabolism and disorders
Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Paraoxonase enzyme and polymorphisms
Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Lipoproteins and Cardiovascular Health
Keywords: hepatic lipase, dyslipidemia, visceral obesity, insulin resistance, dietary fat intake, gender differences, HDL cholesterol, small dense LDL, lipid-lowering drugs, metabolic syndrome, type 2 diabetes, familial combined hyperlipidemia, atherogenic lipoprotein profile
MeSH terms: Diabetes Mellitus, Type 2, Diet, Female, Haplotypes, Humans, Hyperlipidemias, Hyperlipidemia, Familial Combined, Lipase, Lipoproteins, LDL, Liver, Male, Models, Biological, Obesity, Polymorphism, Genetic, Promoter Regions, Genetic, Sex Factors, Genetic Variation

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Hepatic lipase and dyslipidemia: interactions among genetic variants, obesity, gender and diet.

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